A Study Using Medical Records of Danish People With Type 2 Diabetes Comparing Empagliflozin and Glucagon-Like Peptide-1 Receptor Agonists (GLP1-RA) in the Occurrence of Serious Cardiovascular Outcomes

Sponsor
Boehringer Ingelheim
Study ID
NCT03993132
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

The primary research question is to evaluate whether, among patients with type 2 diabetes mellitus (T2D), initiation of empagliflozin changes the adjusted incidence of outcomes compared with initiation of Glucagon-Like Peptide-1 Receptor Agonists (GLP1-RA).

Key Dates

First listed
Jun 20, 2019
Start date
Oct 1, 2018
Status verified
Jun 2023
Primary completion
Jun 16, 2022
Completion
Jun 16, 2022

Study Design

Enrollment
26,774 participants (actual)

Arms

  • Arm: Patients with type 2 diabetes

Primary Outcome Measure

Incidence Rate of Expanded Major Adverse Cardiovascular Event (MACE) Composite Outcome - OT Analysis [ Time Frame: From first initiation of empagliflozin or liraglutide until end of follow-up, up to 6 years. ]

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